Applied and Computational Mathematics (ACM)

Dynamic Iteration Schemes

Dynamic iteration via source coupling

Standard time-integration methods solve transient problems all at once. This may become very inefficient or impossible for large systems of equations. Imaging that such large systems often stem from a coupled problem formulation, where different physical phenomena interact and need to be coupled in order to produce a precise mathematical model.
E.g. highly integrated electric circuits (as in memory chips or CPUs) produce heat, which effects in turn their behavior as electrical system; thus one needs to couple electric and thermal subproblem descriptions. On the one hand, this creates multiple time scales due to different physical phenomena, which demands an efficient treatment, see multirate. On the other hand, in a professional environment one usually has dedicated solvers for the subproblems, which need to be used, and an overall problem formulation is not feasible for any of the involved tools.

For those partitioned problems a dynamic iteration method becomes beneficial or even the sole way-out: it keeps the subproblems separate, solves subproblems sequentially (or in parallel) and iterates until convergence (fixed-point interation). Thus the subproblem's structure can be exploited in the respective integration.

To guarantee or to speed up convergence the time interval of interest is split into a series of windows. Then the time-integration of the windows is applied sequentially and in each window the subproblems are solved iteratively by your favoured method.

Group members working on that field

  • Andreas Bartel
  • Michael Günther

Former and ongoing Projects

Cooperation

Publications



1992

378.

Benter, Thorsten; Becker, Eilhard; Wille, Uta; Rahman, M. M.; Schindler, Ralph N.
The Determination of Rate Constants for the Reactions of Some Alkenes with the NO\(_{3}\) Radical
Berichte der Bunsengesellschaft für physikalische Chemie, 96 (6) :769-775
1992

377.

Benter, Thorsten; Becker, Eilhard; Wille, Uta; Rahman, M. M.; Schindler, Ralph N.
The Determination of Rate Constants for the Reactions of Some Alkenes with the NO3 Radical
Berichte der Bunsengesellschaft für physikalische Chemie, 96 (6) :769-775
1992

376.

Ziebarth, K.; Breidohr, R.; Shestakov, Oleg; Fink, Ewald H.
The X\(_{2}\) \(^{2}\)\(\Pi\)\(_{3/2}\) → X\(_{1}\) \(^{2}\)\(\Pi\)\(_{1/2}\) electronic band systems of lead monohalides in the near infrared
Chemical Physics Letters, 190 (3-4) :271-278
1992

375.

Ziebarth, K.; Breidohr, R.; Shestakov, Oleg; Fink, Ewald H.
The X\(_{2}\) \(^{2}\)\(\Pi\)\(_{3/2}\) → X\(_{1}\) \(^{2}\)\(\Pi\)\(_{1/2}\) electronic band systems of lead monohalides in the near infrared
Chemical Physics Letters, 190 (3-4) :271-278
1992

374.

Ziebarth, K.; Breidohr, R.; Shestakov, Oleg; Fink, Ewald H.
The X2 2Π3/2 → X1 2Π1/2 electronic band systems of lead monohalides in the near infrared
Chemical Physics Letters, 190 (3-4) :271-278
1992

373.

Barone, Vincenzo; Jensen, Per; Minichino, Camilla
Vibro-rotational analysis of Si\(_{2}\)C from an ab initio potential energy surface. A comparison between perturbative and variational methods
Journal of Molecular Spectroscopy, 154 (2) :252-264
1992

372.

Barone, Vincenzo; Jensen, Per; Minichino, Camilla
Vibro-rotational analysis of Si\(_{2}\)C from an ab initio potential energy surface. A comparison between perturbative and variational methods
Journal of Molecular Spectroscopy, 154 (2) :252-264
1992

371.

Barone, Vincenzo; Jensen, Per; Minichino, Camilla
Vibro-rotational analysis of Si2C from an ab initio potential energy surface. A comparison between perturbative and variational methods
Journal of Molecular Spectroscopy, 154 (2) :252-264
1992
1991

370.

Fink, Ewald H.; Setzer, Klaus-Dieter; Ramsay, D. A.; Vervloet, M.
A new band spectrum of BiO in the near-infrared region
Chemical Physics Letters, 179 (1-2) :103-108
1991

369.

Fink, Ewald H.; Setzer, Klaus-Dieter; Ramsay, D. A.; Vervloet, M.
A new band spectrum of BiO in the near-infrared region
Chemical Physics Letters, 179 (1-2) :103-108
1991

368.

Fink, Ewald H.; Setzer, Klaus-Dieter; Ramsay, D. A.; Vervloet, M.
A new band spectrum of BiO in the near-infrared region
Chemical Physics Letters, 179 (1-2) :103-108
1991

367.

Becker, Eilhard; Benter, Thorsten; Kampf, R.; Schindler, Ralph N.; Wille, Uta
A Redetermination of the Rate Constant of the Reaction F + HNO\(_{3}\) → HF + NO\(_{3}\)
Berichte der Bunsengesellschaft für physikalische Chemie, 95 (10) :1168-1173
1991

366.

Becker, Eilhard; Benter, Thorsten; Kampf, R.; Schindler, Ralph N.; Wille, Uta
A Redetermination of the Rate Constant of the Reaction F + HNO\(_{3}\) → HF + NO\(_{3}\)
Berichte der Bunsengesellschaft für physikalische Chemie, 95 (10) :1168-1173
1991

365.

Becker, Eilhard; Benter, Thorsten; Kampf, R.; Schindler, Ralph N.; Wille, Uta
A Redetermination of the Rate Constant of the Reaction F + HNO3 → HF + NO3
Berichte der Bunsengesellschaft für physikalische Chemie, 95 (10) :1168-1173
1991

364.

Jensen, Per; Bunker, Philip R.; Karpfen, Alfred
An ab initio calculation of the nonadiabatic effect on the tunneling splitting in vibrationally excited (HF)\(_{2}\)
Journal of Molecular Spectroscopy, 148 (2) :385-390
1991

363.

Jensen, Per; Bunker, Philip R.; Karpfen, Alfred
An ab initio calculation of the nonadiabatic effect on the tunneling splitting in vibrationally excited (HF)\(_{2}\)
Journal of Molecular Spectroscopy, 148 (2) :385-390
1991

362.

Jensen, Per; Bunker, Philip R.; Karpfen, Alfred
An ab initio calculation of the nonadiabatic effect on the tunneling splitting in vibrationally excited (HF)2
Journal of Molecular Spectroscopy, 148 (2) :385-390
1991

361.

Jensen, Per; Marshall, Mark D.; Bunker, Philip R.; Karpfen, Alfred
An ab initio close-coupling calculation of the lower vibrational energies of the HCl dimer
Chemical Physics Letters, 180 (6) :594-600
1991

360.

Jensen, Per; Marshall, Mark D.; Bunker, Philip R.; Karpfen, Alfred
An ab initio close-coupling calculation of the lower vibrational energies of the HCl dimer
Chemical Physics Letters, 180 (6) :594-600
1991

359.

Jensen, Per; Marshall, Mark D.; Bunker, Philip R.; Karpfen, Alfred
An ab initio close-coupling calculation of the lower vibrational energies of the HCl dimer
Chemical Physics Letters, 180 (6) :594-600
1991

358.

Marshall, Mark D.; Jensen, Per; Bunker, Philip R.
An ab initio close-coupling calculation of the lower vibrational energies of the HF dimer
Chemical Physics Letters, 176 (3-4) :255-260
1991

357.

Marshall, Mark D.; Jensen, Per; Bunker, Philip R.
An ab initio close-coupling calculation of the lower vibrational energies of the HF dimer
Chemical Physics Letters, 176 (3-4) :255-260
1991

356.

Marshall, Mark D.; Jensen, Per; Bunker, Philip R.
An ab initio close-coupling calculation of the lower vibrational energies of the HF dimer
Chemical Physics Letters, 176 (3-4) :255-260
1991

355.

Karpfen, Alfred; Bunker, Philip R.; Jensen, Per
An ab initio study of the hydrogen chloride dimer: the potential energy surface and the characterization of the stationary points
Chemical Physics, 149 (3) :299-309
1991

354.

Karpfen, Alfred; Bunker, Philip R.; Jensen, Per
An ab initio study of the hydrogen chloride dimer: the potential energy surface and the characterization of the stationary points
Chemical Physics, 149 (3) :299-309
1991